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Well fellas im about to become a dad for the first time. My wife’s water just broke. Any tips and advice is greatly appr...
09/18/2026

Well fellas im about to become a dad for the first time. My wife’s water just broke. Any tips and advice is greatly appreciated!

Edit: he is here ! Momma and him are okay!

A 9-year-old boy who has spent nearly his entire summer in the hospital fighting complications from a rare genetic skin ...
09/12/2026

A 9-year-old boy who has spent nearly his entire summer in the hospital fighting complications from a rare genetic skin condition looked into a camera and asked strangers for something heartbreaking:
“Please pray for me.”
Jamison was born with Harlequin ichthyosis, a severe disorder that causes the skin to grow abnormally thick and tight, leaving patients vulnerable to painful cracking, infections and problems regulating body temperature and hydration.
He has lived with it his entire life.
But his mom, Alicia, says what has happened this summer has been the scariest stretch they have ever faced.
“I have been in the hospital for this whole summer,” Jamison says in the video. “I got nothing to do… it doesn’t make me happy.”
Then the 9-year-old says something that is difficult to hear:
“I really am not happy about my life. This is the worst life ever, and it feels like hell.”
And then again:
“Please pray for me.”
Alicia says two days before Jamison recorded that video, his symptoms became so severe that even his pain medications at their maximum prescribed doses were not controlling his pain.
He was crying, vomiting and saying things that broke his mom’s heart.
She says Jamison is also battling two bacterial infections that are taking a tremendous toll on his already fragile body.
“In all of these years going through this I can say this has by far been the scariest and worst experience for the both of us,” Alicia shared. “Mentally, physically, and emotionally.”
The encouraging news is that Jamison is more stable today.
But this family is facing another incredibly difficult moment.
Alicia says she is preparing to sit down with 12 specialists, along with hospice and palliative-care teams, for what she calls a “care moving forward” meeting.
“I’m so not prepared.”
Imagine hearing your 9-year-old tell the world that he is tired of the hospital, tired of hurting and unhappy with the life he is living — and then having to walk into a room with that many doctors to talk about what comes next.
Alicia has also made it clear that she will continue sharing the difficult parts of her son’s journey because this is their reality.
Right now, they don’t need judgment.
They need exactly what Jamison asked for.
Prayer. 💙🙏
Please pray for relief from his pain.
Pray these infections respond to treatment.
Pray for wisdom and compassion from every specialist helping guide his care.
And please leave Jamison a personal message to read here reminding him just how special he really is.
Jamison asked us plainly:
“Please pray for me.”
Let’s make sure this little boy knows people heard him.

Happy birthday to my daughter! Some heartless people won’t congratulate her just because she is different.
09/08/2026

Happy birthday to my daughter!
Some heartless people won’t congratulate her just because she is different.

When baby Jonathan was born, his parents were 𝗌𝗁𝗈𝖼𝗄𝖾𝖽 to learn he had bilateral clubfoot, a condition affecting both fee...
09/04/2026

When baby Jonathan was born, his parents were 𝗌𝗁𝗈𝖼𝗄𝖾𝖽 to learn he had bilateral clubfoot, a condition affecting both feet that had gone unnoticed during pregnancy. 💔

At just five weeks old, Jonathan’s little journey took an unexpected turn, beginning with casts, procedures, and weekly hospital visits. 🏥 Over the following months, he went through 13 casts and three tendon procedures, showing incredible strength with every step. 👣

When his condition turned out to be more complex than expected, his family traveled to another state to find specialized care.

BORN WITH A "TURTLE SHELL" COVERING 75% OF HIS BACK...🐢When James McCallum was born, his parents and doctors were stunne...
09/04/2026

BORN WITH A "TURTLE SHELL" COVERING 75% OF HIS BACK...🐢
When James McCallum was born, his parents and doctors were stunned by an unusual growth covering much of his back. 😔

At just two months old, he was diagnosed with giant congenital melanocytic nevus, a rare skin condition that continued changing as he grew. 💔

While his parents waited for answers, the mole-like mark gradually spread across most of James’s back. As it became thicker, James could no longer lie comfortably on his back. 🙏

😢 A SIMPLE PENCIL TURNED INTO A 𝖭𝖨𝖦𝖧𝖳𝖬𝖠𝖱𝖤...💔 A sweet little moment of joy took an unexpected turn for two-year-old Wren...
09/04/2026

😢 A SIMPLE PENCIL TURNED INTO A 𝖭𝖨𝖦𝖧𝖳𝖬𝖠𝖱𝖤...
💔 A sweet little moment of joy took an unexpected turn for two-year-old Wren Bowell. Like many toddlers, Wren loved coloring and drawing. One evening, she excitedly ran out of her room to show her parents the picture she had just finished.

Then, while running with a pencil in her hand, Wren stumbled. In an instant, the pencil entered near her eye and reached deep 𝗂𝗇𝗌𝗂𝖽𝖾 her head. ✏️💔

😭 A Texas mom fighting terminal cancer has started recording videos for her four children for a reason that is almost un...
09/04/2026

😭 A Texas mom fighting terminal cancer has started recording videos for her four children for a reason that is almost unbearable.
She wants them to remember her voice.
Her face.
Who their mom was.
Samantha Hernandez lives in Magnolia, Texas, and has been fighting stage 4 peripheral T-cell lymphoma for nearly two years.
But recently, Sammie started doing something she had promised herself she wouldn’t do during her cancer fight.
She started making TikToks.
She calls the account “Love Letters From Sammie.”
And when you understand why, these videos hit completely differently.
“To my babies…”
That is how one begins.
Sammie looks into the camera and names them:
Claire. Ben. Asher. Delilah.
Then she explains why she’s recording.
“I want Ben to have videos of me so he can like really see me and really remember me.”
“I want y’all to have my voice that y’all can hear if anything happens.”
Read that again.
This is a mother thinking about a future in which one of her children may be too young to remember what she sounded like.
And yet, even while saying it, Sammie refuses to surrender.
“We’re still in the fight, we’re still in the fight, we’re not giving up.”
But then comes the sentence that exposes the fear underneath all of it:
“I’m scared, we’re running out of time.”
Sammie was 35 and her youngest was only five months old when she was diagnosed.
During her first round of chemotherapy, she suffered a massive hemorrhagic stroke and nearly died.
She survived that, relearned abilities the stroke had taken from her and continued fighting the cancer.
She eventually got encouraging enough results to begin preparing for a stem cell transplant.
Then the lymphoma returned.
Now, after more treatments and clinical trial medications, Sammie says another enormous obstacle stands between her and continuing that fight.
She says her insurance was canceled, she has been denied other coverage and Medicare won’t begin for another five months.
Sammie says doctors have told her untreated cancer could take her life much sooner than that.
So while she fights for access to treatment, she’s also doing something no 37-year-old mother should have to contemplate:
Making sure her children have pieces of their mom if she isn’t here someday to tell them these stories herself.
And these aren’t polished farewell videos.
That’s what makes them so powerful.
She talks about family.
She jokes about her brother getting old.
She tells her kids about the music she loved growing up.
She laughs.
She remembers.
She’s leaving behind the ordinary pieces of herself that children can spend a lifetime wishing they could hear just one more time.
Because Sammie doesn’t want to become only a photograph to her youngest.
She wants him to know her voice.
Her personality.
Her laugh.
His mom.
And despite everything she’s facing, her goal for the future isn’t some enormous milestone.
“I want to be here long enough to see my two year old graduate kindergarten!”
Kindergarten.
That is the finish line this mother is begging for right now.
Jenn, another woman touched personally by this same disease, reached out to me hoping more people would see Sammie’s fight.
I’m glad she did.
Because somewhere tonight, most of us will hear our kids call “Mom” or “Dad” without giving it a second thought.
Sammie is fighting for more days when her children can still call for her—and hear their mom answer back.
So I want to turn the comments over to her.
If Samantha is reading today, what would you tell this mom about the memories she’s making RIGHT NOW—and what would you tell her to help her keep fighting for that kindergarten graduation and beyond?

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